Construction of nondefective adenovirus type 5 bearing a 2.8-kilobase hepatitis B virus DNA near the right end of its genome
about
Mammalian thioredoxin is a direct inhibitor of apoptosis signal-regulating kinase (ASK) 1.Production of viral vectors using recombinase-mediated cassette exchangeCRISPR-Cas9 as a Powerful Tool for Efficient Creation of Oncolytic VirusesAdvances and future challenges in recombinant adenoviral vectored H5N1 influenza vaccinesProduction of adenovirus vectors and their use as a delivery system for influenza vaccines.Effective prevention of thrombocytopenia in mice using adenovirus-mediated transfer of HST-1 (FGF-4) geneAdenovirus-mediated transfer of the HST-1 (FGF4) gene induces increased levels of platelet count in vivo.Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome.Transient gene transfer and expression of Smad7 prevents bleomycin-induced lung fibrosis in miceA histologically distinctive interstitial pneumonia induced by overexpression of the interleukin 6, transforming growth factor beta 1, or platelet-derived growth factor B geneRecombinant adenovirus induces antibody response to hepatitis B virus surface antigen in hamsters.Species D human adenovirus type 9 exhibits better virus-spread ability for antitumor efficacy among alternative serotypes.Adenovirus-mediated gene transfer and expression of human beta-glucuronidase gene in the liver, spleen, and central nervous system in mucopolysaccharidosis type VII mice.Adenoviral protein V promotes a process of viral assembly through nucleophosmin 1.Thermostability/infectivity defect caused by deletion of the core protein V gene in human adenovirus type 5 is rescued by thermo-selectable mutations in the core protein X precursor.Synthesis and processing of human immunodeficiency virus type 1 envelope proteins encoded by a recombinant human adenovirus.Distinctive properties of the hepatitis B virus envelope proteins.Development of a helper-independent human adenovirus vector and its use in the transfer of the herpes simplex virus thymidine kinase gene.Novel RNA family structure of hepatitis B virus expressed in human cells, using a helper-free adenovirus vector.Construction, rescue, and characterization of vectors derived from ovine atadenovirus.Local expression of immunoregulatory IL-12p40 gene prolonged syngeneic islet graft survival in diabetic NOD mice.In vitro dynamic visualization analysis of fluorescently labeled minor capsid protein IX and core protein V by simultaneous detectionEfficient genome replication of hepatitis B virus using adenovirus vector: a compact pregenomic RNA-expression unit.Roles of bone morphogenetic protein type I receptors and Smad proteins in osteoblast and chondroblast differentiation.Efficient production of adenovirus vector lacking genes of virus-associated RNAs that disturb cellular RNAi machinery.The bone morphogenetic protein type Ib receptor is a major mediator of glial differentiation and cell survival in adult hippocampal progenitor cell culture.Induction of differentiation in normal human keratinocytes by adenovirus-mediated introduction of the eta and delta isoforms of protein kinase C.High-level expression by tissue/cancer-specific promoter with strict specificity using a single-adenoviral vector.Inhibition of rat vascular smooth muscle proliferation in vitro and in vivo by bone morphogenetic protein-2.Simultaneous on/off regulation of transgenes located on a mammalian chromosome with Cre-expressing adenovirus and a mutant loxP.Gene targeting with a replication-defective adenovirus vector.ASK1 inhibits astroglial development via p38 mitogen-activated protein kinase and promotes neuronal differentiation in adult hippocampus-derived progenitor cells.Short insertions in the partner strands greatly enhance the discriminating power of DNA heteroduplex analysis: resolution of HLA-DQB1 polymorphisms.Enhancement of retrovirus-mediated gene transduction efficiency by transient overexpression of the amphotropic receptor, GLVR-2.Efficient gene activation in mammalian cells by using recombinant adenovirus expressing site-specific Cre recombinase.Preferable sites and orientations of transgene inserted in the adenovirus vector genome: The E3 site may be unfavorable for transgene position.
P2860
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P2860
Construction of nondefective adenovirus type 5 bearing a 2.8-kilobase hepatitis B virus DNA near the right end of its genome
description
1985 nî lūn-bûn
@nan
1985年の論文
@ja
1985年論文
@yue
1985年論文
@zh-hant
1985年論文
@zh-hk
1985年論文
@zh-mo
1985年論文
@zh-tw
1985年论文
@wuu
1985年论文
@zh
1985年论文
@zh-cn
name
Construction of nondefective a ...... ar the right end of its genome
@en
type
label
Construction of nondefective a ...... ar the right end of its genome
@en
prefLabel
Construction of nondefective a ...... ar the right end of its genome
@en
P2093
P2860
P1433
P1476
Construction of nondefective a ...... ar the right end of its genome
@en
P2093
P2860
P304
P407
P577
1985-06-01T00:00:00Z